P38S (p.Pro38Ser) variant of CALCB (P10092)
P38S (p.Pro38Ser) in CALCB (P10092) is a missense change. The available variant effect predictions contribute to a CATVariant prioritization score of 0.16 / 1. The record also includes population frequency data and structural context.
P38S (p.Pro38Ser) variant details
- p.Pro38Ser
- cosmic curated COSV60834
- TOPMed rs1051094271
- gnomAD rs1051094271
- Missense
- Variant Prioritization Score for Impact Estimate 0.157
- REVEL 0.09
- CADD 8.87
- PolyPhen-2 0.00
- SIFT 0.69
- Most common in the African/African-American population (allele frequency 4.8e-05)
- Structural context available